S U T H E R L A N D E T AI.,
Photoreactivation of Pyrimidine Dimers in the DNA of Normal and Xeroderma Pigmentosum Cells? Betsy M. Sutherland,* Rowena Oliver, Charles 0. Fuselier, and John C. Sutherland
ABSTRACT: Photoproducts formed in the D N A of human cells irradiated with ultraviolet light (uv) were identified as cyclobutyl pyrimidine dimers by their chromatographic mobility, reversibility to monomers upon short wavelength uv irradiation, and comparison of the kinetics of this monomerization with that of authentic cis-syn thymine-thymine dimers prepared by irradiation of thymine in ice. The level of cellular photoreactivation of these dimers reflects the level of photoreactivating enzyme measured in cell extracts.
Action spectra for cellular dimer photoreactivation in the xeroderma pigmentosum line XP12BE agree in range (300 nm to a t least 577 nm) and maximum (near 400 nm) with that for photoreactivation by purified human photoreactivating enzyme. Normal human cells can also photoreactivate dimers in their DNA. The action spectrum for the cellular monomerization of dimers is similar to that for photoreactivation by the photoreactivating enzyme in extracts of normal human fibroblasts.
T h e photoreactivating enzyme repairs ultraviolet light induced damage in D N A by monomerizing pyrimidine dimers in a light-dependent reaction (Rupert, 1962). The enzyme binds to the dimer-containing DNA, probably a t the site of a dimer [the name cyclobutadipyrimidine has been proposed for the dimer by Madden et al., 1973 and Cohn et al., 19741. On absorption of a photon in the range 300-600 n m , the enzyme catalyzes the photolysis of the cyclobutane ring, producing two monomer pyrimidines and restoring biological activity to the D N A (Setlow and Setlow, 1963). The specific and exclusive action of the enzyme on pyrimidine dimers (Setlow and Setlow. 1963) make it of potential importance as an analytical tool: if ultraviolet light induced biological damage can be prevented in a true photoenzymatic reaction, pyrimidine dimers were a major contributor to the production of that damage. In human cells the evaluation of the role of pyrimidine dimers in the induction of skin cancer by ultraviolet light (Epstein, 1971) is a case of special interest. Since a photoreactivating enzyme has only recently been isolated from mammalian cells (Sutherland, 1974; Sutherland et al., 1974), its role in cellular repair phenomena is not yet clear. Sutherland et al. (1975) presented data showing that the cells of the xeroderma pigmentosum line XP12BE (Robbins et al., 1974) could photoreactivate dimers in its DNA. Since previous data on cellular photoreactivation have been contradictory (see Sutherland. 1974, for a discussion), we have examined this celliilar photoreactivation phenomenon further. We show here that the D N A photoproduct from uv-irradiated human cells which can be removed from the D N A by photoreactivation is the cis-syn cyclobutyl pyrimidine
dimer, that the extent of cellular photoreactivation of dimers reflects the level of photoreactivating enzyme measured in cell extracts, and that the action spectrum for photoreactivation by the xeroderma line XP12BE is similar in range and maximum to that measured for purified human photoreactivating enzyme (Sutherland et al., 1974; Sutherland and Sutherland, 1975). W e also find that normal human cells can photoreactivate dimers in their DNA, and that the action spectrum for dimer photoreactivation by these cells is similar to that measured for in vitro photoreactivation by the photoreactivating enzyme in extracts of these cells.
From the Department of Molecular Biology and Biochemistry, Lniversity of California, Irvine, California 92664 (B.M.S.. R.O., and C.O.F.). and the Department of Physiology, California College of Medicine, University of California, Irvine, California 92664 (J.C.S.). Receiced July I / , 1975. This research was supported by grants from the American Cancer Society and National Institutes of Health and a Research Career Development award to B.M.S., and by grants from the National Institutes of Health and Atomic Energy Commission to J.C.S
402
BIOCHEMISTRY.
VOL.
15,
NO.
2, 1976
Experimental Procedures
Cells. The xeroderma line XP12BE (Jay Tim, C R L 1223) was obtained from the American Type Culture Collection; the xeroderma line Sally G was the gift of Dr. James Regan, Oak Ridge National Laboratory. A human embryonic skin and muscle line ( H E S M ) was purchased from Flow Laboratories. Cells were grown in Dulbecco’s modified Eagle’s medium supplemented with 20% fetal calf serum (Flow Laboratories) and contained penicillin ( 1 00 units/ml) and streptomycin (20 kg/mI). Cells were grown routinely in T75 flasks (Falcon Laboratories). For radioactive labeling of the D N A , cells were seeded from one T75 flask into small culture dishes (35 mni diameter). After 12 hr growth, radioactive medium [Dulbecco’s modified Eagle’s medium containing 6% dialyzed fetal calf serum and 5 wCi/ml of [‘Hlthymidine (Schwarz/ Mann)] was added and the cells were grown for 24 hr. The labeling medium was removed and the cells were washed two times with I ml of 0.15 M NaCI; finally 1 ml of 0.1 5 M NaCl was added to the dish. Irradiation of Cells. Cells in small culture dishes were exposed to 254-nm radiation from a 15-W low-pressure mercury arc. Exposure rates were measured with a Jagger meter (Jagger, 1961) which had been calibrated using a Hewlett Packard thermopile. Photoreactivation experiments were carried out in two ways. (1) Immediately after irradiation a t 254 nm, the dishes containing the cells were placed in a Plexiglas box and exposed to broad spectrum
PHOTOREACTIVATION OF PYRIMIDINE DIMERS IN HUMAN CELLS
white light from a 60-W frosted bulb at 20 cm distance. (2) For action spectrum measurements, the cells were irradiated at 254 nm as described above, then scraped into the overlying saline and transferred to a Pyrex tube which was inserted into the sample chamber of a high intensity monochromator. Dimer Monomerization. Dimers were monomerized with 248-nm radiation from a high intensity monochromator (Johns and Rauth, 1965a,b). Samples were stirred during irradiation and, in the case of the solution of synthetic dimers, absorbance at 264 nm was monitored with a Zeiss spectrophotometer which is an integral part of the irradiation facility (Johns, 1967). Action spectra were also measured with radiation from the high intensity monochromator Second-order uv radiation was removed by a 3 in. diameter 0.25 in. thick Pyrex plate between the mercury arc and the entrance slit and, in the case of the 577-nm line, a yellow Corning filter was placed in front of the sample. Samples were placed in 6-mm diameter Pyrex test tubes which were suspended in a 2 in. diameter cylindrical irradiation chamber, the inner walls of which were covered with barium sulfate high reflectance paint (Middleton and Sanders, 1953). The monochromatic beam entered through a 0.25 X 1.25 in. slit in the side of the irradiation chamber and was reflected diffusely from the walls of the chamber, thus reducing focusing effects caused by the test tube. Fluences of the radiation entering the irradiation chamber were adjusted by varying the ganged entrance and exit slits of the monochromator to produce equal numbers of photons during the period of irradiation for each of the different wavelengths. Fluences were measured with the photoelectric cell which is an integral part of the facility (Johns, 1967). The photocell was calibrated with a Hewlett Packard thermopile. Dimer Analysis. After uv and/or photoreactivating light treatment, cells were killed by the addition of an equal volume of 20% trichloroacetic acid, mixed, and placed on ice. The cell suspensions were centrifuged for 15 min at 15 000 rpm in the SS34 rotor of the Sorvall RC2B centrifuge. The tubes were drained briefly to remove the last traces of the saline solution, 0.15 ml of 98% formic acid was added to each tube and the tubes were sealed. Samples were hydrolyzed a t 175OC for 35-40 min, opened, dried, and chromatographed on Whatman No. 1 paper or cellulose thin layers (Brinkman) in 1-butanol-acetic acid-water (40:6:15, v/v). The chromatograms were cut into 1-cm (for paper) or 0.5cm (for thin-layer) strips, eluted with 0.5 ml water, and counted in a dioxane-based scintillation fluid (containing 120 g of naphthalene and 3.0 g of 2,5-bis (S-tert-butyl-2benzoazoy1)thiophene per 1.) in a LKB scintillation counter. Cis-Syn Thymine- Thymine Dimers. Thymine dimers were prepared by irradiating a frozen aqueous thymine solution according to the technique of Beukers and Berends (1960). The irradiated solution was thawed and filtered to collect crystals. The crystals were dried at 6OoC and extracted in absolute ethanol to remove unreacted thymine. The identity of the dimers was confirmed by three criteria. First, upon 254-nm irradiation in solution the dimer was converted to a product which had an absorption maximum at about 264 nm and a chromatographic mobility (in butanol-acetic acid-water) characteristic of thymine (Setlow and Setlow, 1962). Nuclear magnetic resonance ( N M R ) spectroscopy indicated a shift in the signal of the vinyl proton of thymine from 6 3.5 to 1.85 after dimerization. The identity of the dimer product as the cis-syn type (also
---
FRACTION
FIGURE 1: Radioactivity profile of chromatogram of a hydrolysate of
HESM cells. Cells were labeled with [3H]thymidine,exposed to ultraviolet light (A),or given no uv treatment (0),killed by the addition of trichloroacetic acid, and subjected to formic acid hydrolysis. The samples were dried, chromatographed in 1-butanol-acetic acid-water (40: 6:15) on Whatman No. 1 paper, and counted. Fractions 8-10 of the chromatogram of the irradiated DNA were eluted and pooled.
formed in uv-irradiated DNA) (Weinblum and Johns, 1966) was established by infrared analysis of KBr pellet of the product: the spectrum was identical with that obtained for the cis-syn thymine dimer by Weinblum and Johns (1966). Photoreactivating Enzyme. Cell extracts were prepared by washing a T75 flask of cells twice with 0.15 M NaCl (60 ml), scraping them into 2 ml of 0.15 M NaCl, centrifuging at 5000 rpm for 10 min in the SE12 rotor of the RC2B centrifuge, rinsing with 2.0 ml of 0.15 M NaCl, centrifuging as before, and resuspending in buffer E (10 m M Tris (pH 7.0), 0.1 m M dithiothreitol, and 0.1 m M EDTA). Cells were sonicated for 45 sec in a Kontes sonicator a t a power setting of 6-7. Photoreactivating enzyme activity was measured by the method of Sutherland and Chamberlin (1 973); units of enzyme activity are given in pmol per mg hr. Protein concentrations were determined by the Lowry method (Lowry et al., 1951). Results Ultraviolet irradiation of D N A in intact eucaryotic cells can result in a complex array of photoproducts (see, for example, Sutherland et al., 1968). Since the only known substrate for the photoreactivating enzyme is the pyrimidine dimer, it is important to measure accurately D N A dimer content; if photoproducts other than dimers appeared in the dimer region of the chromatogram, their disappearance might be mistaken for true photoreactivation. We have thus examined the. identity of the photoproduct appearing in the dimer region of chromatograms of hydrolysates of uv-irradiated [3H]thymidine-labeled human cells. A radioactivity profile of such a chromatogram is shown in Figure 1; a profile of a chromatogram of unirradiated D N A is also shown in Figure 1. The photoproduct appearing in fractions 8-10 was eluted from the chromatogram and aliquots were given increasing exposures to 248nm radiation from a high intensity monochromator. Profiles of chromatograms of the initial (no radiation), an intermeBIOCHEMISTRY, VOL.
15, NO. 2, 1976
403
S1J I H E R I A N I )
ET AIi
50
rable I e5
-x
Excision Renair
a
0 0
-
I-
1 100
0 0 a a 5c
L
n 0
*. 20
10
FPACTION
F l G l l R E 2: Conversion of “dimer” to thymine by 248-nm irradiation. Pooled “dimer” peak from the chromatogram of uv-irradiated HESM DNA (see Figure I ) was rechromatographed on Brinkman cellulose thin layers on I-butanol-acetic acid water (40:6:15) without exposure to light (top). after 4-min exposure to 248 n m (middle; right axis), or after 16-min exposure (bottom). The 218 nirl radiation was delivered at a rate of 2 X 10l6 photons/sec
0
2 4 IRRADIATION
6
(5)
XPl2BF Sally G
i2d
-
1 iaition c’f Cellular Dimers Photoreactivatedb in .
5 niin
-
7 0 min
0 72 0 22 0 15 _ _ _- ___ - .- - . 0 Photoreactivating en7yme levels were compared to those in nor mal cells (HESM), taken as l @ O % These cell? confamed photoreactivating enzyme at a Fpecific activity of 6UO 6 2 5 prnol per mg per hr b Fraction of dimers photoreactivated wa? calculated by dividing the dimer content of cellq evposed t o photoreactivating light by the \aliie for cellq kept in the dark for the same period c P h o t o r e a ~ t i vating enzyme levels below 20% and dirner photorcartivation mea surements heIou 0 10 are subject t o uncertainty d Robbins et al (1974) . - e- J Regan. _ _penonal communication
>
ta
Cell Line
Photo reactivating Fn7vtne 4ctivitya (’7)
8
(mid
FIGLRE 3 : Kinetics of the conversion of the radioactive labeled photoproducts obtained as shown in Figure I and the monomerization of authentic pvrimidine dimers plotted as a function of time of exposure to 248-nm radiation. The incident fluencp was 2 X 10l6 photons/sec. The disappearance of the authentic dimers was measured by plotting ,4, A (0)where A was the absorbance observed after a given fluence and ,4, was the limiting absorbance achieved after extensive exposure. The percent unconverted radioactive photoproduct (e) was measured chromatographically. The two lines were detFrmined by the method of least squares
diate (4 min of 248-nm radiation), and the final (16 min) aliquots are shown in Figure 2, top, middle, and bottom. respectively. We have also compared the kinetics of monomerization of authentic thymine -thymine dimers with that of the photoproduct from uv-irradiated human cells. Figure 3 shows that the human DNA photoproduct is converted from a product with an R/ of 0.27 [cf. Rj.of 0.3 for thymine---thy.mine dimers (Setlow and Carrier, 1966)J to one of 0.58 [ R f of thymine = 0.6 (Setlow and Carrier, 1966)] with the same kinetics as the conversion of thymine dimer to monomeric thymine. We thus conclude that the photoproduct from uv-irradiated human DNA- -which has an R,- of about 0.27 in butanol---aceticacid-water, i s converted to a product of Rf of thymine, and is monomerized with kinetics similar to that of authentic thymine dimer--- i s indeed a cyclobutyl pyrimidine dimer. Leuelr ef Dinier Photnreartiuation and Pfrotoren.tiraf-
Photoreactivation of Pyrimidine Dimers in the DNA of Normal and Xeroderma Pigmentosum Cells? Betsy M. Sutherland,* Rowena Oliver, Charles 0. Fuselier, and John C. Sutherland
ABSTRACT: Photoproducts formed in the D N A of human cells irradiated with ultraviolet light (uv) were identified as cyclobutyl pyrimidine dimers by their chromatographic mobility, reversibility to monomers upon short wavelength uv irradiation, and comparison of the kinetics of this monomerization with that of authentic cis-syn thymine-thymine dimers prepared by irradiation of thymine in ice. The level of cellular photoreactivation of these dimers reflects the level of photoreactivating enzyme measured in cell extracts.
Action spectra for cellular dimer photoreactivation in the xeroderma pigmentosum line XP12BE agree in range (300 nm to a t least 577 nm) and maximum (near 400 nm) with that for photoreactivation by purified human photoreactivating enzyme. Normal human cells can also photoreactivate dimers in their DNA. The action spectrum for the cellular monomerization of dimers is similar to that for photoreactivation by the photoreactivating enzyme in extracts of normal human fibroblasts.
T h e photoreactivating enzyme repairs ultraviolet light induced damage in D N A by monomerizing pyrimidine dimers in a light-dependent reaction (Rupert, 1962). The enzyme binds to the dimer-containing DNA, probably a t the site of a dimer [the name cyclobutadipyrimidine has been proposed for the dimer by Madden et al., 1973 and Cohn et al., 19741. On absorption of a photon in the range 300-600 n m , the enzyme catalyzes the photolysis of the cyclobutane ring, producing two monomer pyrimidines and restoring biological activity to the D N A (Setlow and Setlow, 1963). The specific and exclusive action of the enzyme on pyrimidine dimers (Setlow and Setlow. 1963) make it of potential importance as an analytical tool: if ultraviolet light induced biological damage can be prevented in a true photoenzymatic reaction, pyrimidine dimers were a major contributor to the production of that damage. In human cells the evaluation of the role of pyrimidine dimers in the induction of skin cancer by ultraviolet light (Epstein, 1971) is a case of special interest. Since a photoreactivating enzyme has only recently been isolated from mammalian cells (Sutherland, 1974; Sutherland et al., 1974), its role in cellular repair phenomena is not yet clear. Sutherland et al. (1975) presented data showing that the cells of the xeroderma pigmentosum line XP12BE (Robbins et al., 1974) could photoreactivate dimers in its DNA. Since previous data on cellular photoreactivation have been contradictory (see Sutherland. 1974, for a discussion), we have examined this celliilar photoreactivation phenomenon further. We show here that the D N A photoproduct from uv-irradiated human cells which can be removed from the D N A by photoreactivation is the cis-syn cyclobutyl pyrimidine
dimer, that the extent of cellular photoreactivation of dimers reflects the level of photoreactivating enzyme measured in cell extracts, and that the action spectrum for photoreactivation by the xeroderma line XP12BE is similar in range and maximum to that measured for purified human photoreactivating enzyme (Sutherland et al., 1974; Sutherland and Sutherland, 1975). W e also find that normal human cells can photoreactivate dimers in their DNA, and that the action spectrum for dimer photoreactivation by these cells is similar to that measured for in vitro photoreactivation by the photoreactivating enzyme in extracts of these cells.
From the Department of Molecular Biology and Biochemistry, Lniversity of California, Irvine, California 92664 (B.M.S.. R.O., and C.O.F.). and the Department of Physiology, California College of Medicine, University of California, Irvine, California 92664 (J.C.S.). Receiced July I / , 1975. This research was supported by grants from the American Cancer Society and National Institutes of Health and a Research Career Development award to B.M.S., and by grants from the National Institutes of Health and Atomic Energy Commission to J.C.S
402
BIOCHEMISTRY.
VOL.
15,
NO.
2, 1976
Experimental Procedures
Cells. The xeroderma line XP12BE (Jay Tim, C R L 1223) was obtained from the American Type Culture Collection; the xeroderma line Sally G was the gift of Dr. James Regan, Oak Ridge National Laboratory. A human embryonic skin and muscle line ( H E S M ) was purchased from Flow Laboratories. Cells were grown in Dulbecco’s modified Eagle’s medium supplemented with 20% fetal calf serum (Flow Laboratories) and contained penicillin ( 1 00 units/ml) and streptomycin (20 kg/mI). Cells were grown routinely in T75 flasks (Falcon Laboratories). For radioactive labeling of the D N A , cells were seeded from one T75 flask into small culture dishes (35 mni diameter). After 12 hr growth, radioactive medium [Dulbecco’s modified Eagle’s medium containing 6% dialyzed fetal calf serum and 5 wCi/ml of [‘Hlthymidine (Schwarz/ Mann)] was added and the cells were grown for 24 hr. The labeling medium was removed and the cells were washed two times with I ml of 0.15 M NaCI; finally 1 ml of 0.1 5 M NaCl was added to the dish. Irradiation of Cells. Cells in small culture dishes were exposed to 254-nm radiation from a 15-W low-pressure mercury arc. Exposure rates were measured with a Jagger meter (Jagger, 1961) which had been calibrated using a Hewlett Packard thermopile. Photoreactivation experiments were carried out in two ways. (1) Immediately after irradiation a t 254 nm, the dishes containing the cells were placed in a Plexiglas box and exposed to broad spectrum
PHOTOREACTIVATION OF PYRIMIDINE DIMERS IN HUMAN CELLS
white light from a 60-W frosted bulb at 20 cm distance. (2) For action spectrum measurements, the cells were irradiated at 254 nm as described above, then scraped into the overlying saline and transferred to a Pyrex tube which was inserted into the sample chamber of a high intensity monochromator. Dimer Monomerization. Dimers were monomerized with 248-nm radiation from a high intensity monochromator (Johns and Rauth, 1965a,b). Samples were stirred during irradiation and, in the case of the solution of synthetic dimers, absorbance at 264 nm was monitored with a Zeiss spectrophotometer which is an integral part of the irradiation facility (Johns, 1967). Action spectra were also measured with radiation from the high intensity monochromator Second-order uv radiation was removed by a 3 in. diameter 0.25 in. thick Pyrex plate between the mercury arc and the entrance slit and, in the case of the 577-nm line, a yellow Corning filter was placed in front of the sample. Samples were placed in 6-mm diameter Pyrex test tubes which were suspended in a 2 in. diameter cylindrical irradiation chamber, the inner walls of which were covered with barium sulfate high reflectance paint (Middleton and Sanders, 1953). The monochromatic beam entered through a 0.25 X 1.25 in. slit in the side of the irradiation chamber and was reflected diffusely from the walls of the chamber, thus reducing focusing effects caused by the test tube. Fluences of the radiation entering the irradiation chamber were adjusted by varying the ganged entrance and exit slits of the monochromator to produce equal numbers of photons during the period of irradiation for each of the different wavelengths. Fluences were measured with the photoelectric cell which is an integral part of the facility (Johns, 1967). The photocell was calibrated with a Hewlett Packard thermopile. Dimer Analysis. After uv and/or photoreactivating light treatment, cells were killed by the addition of an equal volume of 20% trichloroacetic acid, mixed, and placed on ice. The cell suspensions were centrifuged for 15 min at 15 000 rpm in the SS34 rotor of the Sorvall RC2B centrifuge. The tubes were drained briefly to remove the last traces of the saline solution, 0.15 ml of 98% formic acid was added to each tube and the tubes were sealed. Samples were hydrolyzed a t 175OC for 35-40 min, opened, dried, and chromatographed on Whatman No. 1 paper or cellulose thin layers (Brinkman) in 1-butanol-acetic acid-water (40:6:15, v/v). The chromatograms were cut into 1-cm (for paper) or 0.5cm (for thin-layer) strips, eluted with 0.5 ml water, and counted in a dioxane-based scintillation fluid (containing 120 g of naphthalene and 3.0 g of 2,5-bis (S-tert-butyl-2benzoazoy1)thiophene per 1.) in a LKB scintillation counter. Cis-Syn Thymine- Thymine Dimers. Thymine dimers were prepared by irradiating a frozen aqueous thymine solution according to the technique of Beukers and Berends (1960). The irradiated solution was thawed and filtered to collect crystals. The crystals were dried at 6OoC and extracted in absolute ethanol to remove unreacted thymine. The identity of the dimers was confirmed by three criteria. First, upon 254-nm irradiation in solution the dimer was converted to a product which had an absorption maximum at about 264 nm and a chromatographic mobility (in butanol-acetic acid-water) characteristic of thymine (Setlow and Setlow, 1962). Nuclear magnetic resonance ( N M R ) spectroscopy indicated a shift in the signal of the vinyl proton of thymine from 6 3.5 to 1.85 after dimerization. The identity of the dimer product as the cis-syn type (also
---
FRACTION
FIGURE 1: Radioactivity profile of chromatogram of a hydrolysate of
HESM cells. Cells were labeled with [3H]thymidine,exposed to ultraviolet light (A),or given no uv treatment (0),killed by the addition of trichloroacetic acid, and subjected to formic acid hydrolysis. The samples were dried, chromatographed in 1-butanol-acetic acid-water (40: 6:15) on Whatman No. 1 paper, and counted. Fractions 8-10 of the chromatogram of the irradiated DNA were eluted and pooled.
formed in uv-irradiated DNA) (Weinblum and Johns, 1966) was established by infrared analysis of KBr pellet of the product: the spectrum was identical with that obtained for the cis-syn thymine dimer by Weinblum and Johns (1966). Photoreactivating Enzyme. Cell extracts were prepared by washing a T75 flask of cells twice with 0.15 M NaCl (60 ml), scraping them into 2 ml of 0.15 M NaCl, centrifuging at 5000 rpm for 10 min in the SE12 rotor of the RC2B centrifuge, rinsing with 2.0 ml of 0.15 M NaCl, centrifuging as before, and resuspending in buffer E (10 m M Tris (pH 7.0), 0.1 m M dithiothreitol, and 0.1 m M EDTA). Cells were sonicated for 45 sec in a Kontes sonicator a t a power setting of 6-7. Photoreactivating enzyme activity was measured by the method of Sutherland and Chamberlin (1 973); units of enzyme activity are given in pmol per mg hr. Protein concentrations were determined by the Lowry method (Lowry et al., 1951). Results Ultraviolet irradiation of D N A in intact eucaryotic cells can result in a complex array of photoproducts (see, for example, Sutherland et al., 1968). Since the only known substrate for the photoreactivating enzyme is the pyrimidine dimer, it is important to measure accurately D N A dimer content; if photoproducts other than dimers appeared in the dimer region of the chromatogram, their disappearance might be mistaken for true photoreactivation. We have thus examined the. identity of the photoproduct appearing in the dimer region of chromatograms of hydrolysates of uv-irradiated [3H]thymidine-labeled human cells. A radioactivity profile of such a chromatogram is shown in Figure 1; a profile of a chromatogram of unirradiated D N A is also shown in Figure 1. The photoproduct appearing in fractions 8-10 was eluted from the chromatogram and aliquots were given increasing exposures to 248nm radiation from a high intensity monochromator. Profiles of chromatograms of the initial (no radiation), an intermeBIOCHEMISTRY, VOL.
15, NO. 2, 1976
403
S1J I H E R I A N I )
ET AIi
50
rable I e5
-x
Excision Renair
a
0 0
-
I-
1 100
0 0 a a 5c
L
n 0
*. 20
10
FPACTION
F l G l l R E 2: Conversion of “dimer” to thymine by 248-nm irradiation. Pooled “dimer” peak from the chromatogram of uv-irradiated HESM DNA (see Figure I ) was rechromatographed on Brinkman cellulose thin layers on I-butanol-acetic acid water (40:6:15) without exposure to light (top). after 4-min exposure to 248 n m (middle; right axis), or after 16-min exposure (bottom). The 218 nirl radiation was delivered at a rate of 2 X 10l6 photons/sec
0
2 4 IRRADIATION
6
(5)
XPl2BF Sally G
i2d
-
1 iaition c’f Cellular Dimers Photoreactivatedb in .
5 niin
-
7 0 min
0 72 0 22 0 15 _ _ _- ___ - .- - . 0 Photoreactivating en7yme levels were compared to those in nor mal cells (HESM), taken as l @ O % These cell? confamed photoreactivating enzyme at a Fpecific activity of 6UO 6 2 5 prnol per mg per hr b Fraction of dimers photoreactivated wa? calculated by dividing the dimer content of cellq evposed t o photoreactivating light by the \aliie for cellq kept in the dark for the same period c P h o t o r e a ~ t i vating enzyme levels below 20% and dirner photorcartivation mea surements heIou 0 10 are subject t o uncertainty d Robbins et al (1974) . - e- J Regan. _ _penonal communication
>
ta
Cell Line
Photo reactivating Fn7vtne 4ctivitya (’7)
8
(mid
FIGLRE 3 : Kinetics of the conversion of the radioactive labeled photoproducts obtained as shown in Figure I and the monomerization of authentic pvrimidine dimers plotted as a function of time of exposure to 248-nm radiation. The incident fluencp was 2 X 10l6 photons/sec. The disappearance of the authentic dimers was measured by plotting ,4, A (0)where A was the absorbance observed after a given fluence and ,4, was the limiting absorbance achieved after extensive exposure. The percent unconverted radioactive photoproduct (e) was measured chromatographically. The two lines were detFrmined by the method of least squares
diate (4 min of 248-nm radiation), and the final (16 min) aliquots are shown in Figure 2, top, middle, and bottom. respectively. We have also compared the kinetics of monomerization of authentic thymine -thymine dimers with that of the photoproduct from uv-irradiated human cells. Figure 3 shows that the human DNA photoproduct is converted from a product with an R/ of 0.27 [cf. Rj.of 0.3 for thymine---thy.mine dimers (Setlow and Carrier, 1966)J to one of 0.58 [ R f of thymine = 0.6 (Setlow and Carrier, 1966)] with the same kinetics as the conversion of thymine dimer to monomeric thymine. We thus conclude that the photoproduct from uv-irradiated human DNA- -which has an R,- of about 0.27 in butanol---aceticacid-water, i s converted to a product of Rf of thymine, and is monomerized with kinetics similar to that of authentic thymine dimer--- i s indeed a cyclobutyl pyrimidine dimer. Leuelr ef Dinier Photnreartiuation and Pfrotoren.tiraf-
